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32篇 您的检索式:作者名="avidan N"
    题名 作者 年代 出处 被引量
1The trace amine receptor 4gene is not associated with schizophrenia in a sample linked to chromosome 6q23显示文摘Amann D Avidan N Kanyas K 2006Mol Psychiatry2006,11,2:1
2Natural video matting using camera arrays 显示文摘Joshi N Matusik W Avidan S 2006ACM Transactions on Graphics2006,25,3:1
3The UDP-N- acetylglueosamine 2-epimerase/N-aeetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy 显示文摘Eisenberg I Avidan N Potikha T 2001Nat Genet2001,29,:1
4Machanisms for evolving hypervariability: the case of conopeptides 显示文摘CONTICELLO S G GILAD Y AVIDAN N 2001Mol Biol Evol2001,18,2:1
5The UDP-N- acetylglucosamine 2-epimerase/N-acetyhnannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy 显示文摘Eisenberg I Avidan N Potikha T 2001Nat Genet2001,29,1:1
6CATSPER2, a human autosomal nonsyndromic male infertility gene显示文摘Avidan N Tamary H Dgany O 2003Eur J Hum Genet2003,11,7:1
7Opposing effects of the HLADRB1 s 0301-DQB1 * 0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel 显示文摘Benedek G Papema T Avidan N 2010Genes Immun2010,11,5:1
8Protein content and composition of leaves and shoot bark in relation to alternate bearing of olive trees 显示文摘LAVEE S AVIDAN N 1994Acta Hortic1994,356,:1
9The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy显示文摘Eisenberg I Avidan N Potikha T 2001Nat Genet2001,29,1:1
10The UDP-N -acetylglucosamine 2-epimerase/N-acetylman nosamine kinase gene is mutated in recessive hereditary inclusion body myopathy显示文摘Eisenberg I Avidan N Potikha T 2001Nat Genet2001,29,1:1
11Possible juvenile- rela ted proteins in olive tree tissues显示文摘Gar cia J L Avidan N T ronco so A 2000Scientia Hort2000,85,:1
12Congenital dyserythropoietic anemia type Ⅰ is caused by mutations in codanin-1显示文摘Dgany O Avidan N Delaunay J 2002Am J Hum Genet2002,71,6:1
13Changes in brainnatriuretic peptide concentrations following open cardiac sur-gery with cardioplegic cardiac arrest显示文摘Avidan MSI Meehan N Ponte J 2001Clin Chim Acta2001,303,12:1
14A missense mutation in a highly conserved region of CASQ2is associated with autosomal recessive catecholamine-inducedpolymorphic ventricular tachycardia in Bedouin families fromIsrael显示文摘Lahat H Pras E Olender T Avidan N Ben-Asher E Man O etal 2001Am J Hum Genet2001,69,6:1
15The implications of HIV for the anaesthetist and the intensivist 显示文摘Avidan MS Jones N Pozniak AL 2000Anaesthesia2000,55,4:1
16The UDP N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy显示文摘Eisenberg I Avidan N Potikha T 2001Nat Genet2001,29,:1
17Translation towards personalized medicine in Multiple Sclerosis显示文摘Miller A Avidan N Tzunz-Henig N 2008J Neurol Sci2008,274,:1
18Phenolic acids-possible involvement in regulating growth and alternate fruiting in olive trees显示文摘Lavee S Harshemesh H Avidan N 1986Acta Hortic1986,179,:1
19The UDP-N- acetylglucosamine 2-epimerase/N-acetyl- mannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy 显示文摘Eisenberg I Avidan N Potikha T 2001Nat Genet2001,29,:1
20Insulin-like growth factorbinding protein 7 regulates keratinocyte proliferation, differentiation and apoptosis 显示文摘Nousbeck J Sarig 0 avidan N 2010J Invest Dennatol2010,130,2:1
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